A Multisite Randomized Controlled Trial of a Patient-Centered Ventricular Assist Device Decision Aid (VADDA Trial)

被引:27
|
作者
Kostick, Kristin M. [1 ]
Bruce, Courtenay R. [1 ]
Minard, Charles G. [2 ]
Volk, Roberti. [3 ]
Civitello, Andrew [4 ]
Krim, Selim R. [5 ]
Horstmanshof, Douglas [6 ]
Thohan, Vinay [7 ]
Loebe, Matthias [8 ]
Hanna, Mazen [9 ]
Bruckner, Brian A. [10 ]
Blumenthal-Barby, J. S. [1 ]
Estep, Jerry D. [9 ]
机构
[1] Baylor Coll Med, Ctr Med Eth & Hlth Policy, Houston, TX 77030 USA
[2] Baylor Coll Med, Dan L Duncan Inst Clin & Translat Res, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Hlth Serv Res, Houston, TX 77030 USA
[4] Baylor Coll Med, Texas Heart Inst, Houston, TX 77030 USA
[5] Ochsner Clin Fdn, New Orleans, LA USA
[6] Integris Hlth, Oklahoma City, OK USA
[7] Aurora St Lukes Med Ctr, Milwaukee, WI USA
[8] Univ Miami, Miller Sch Med, Miami, FL 33136 USA
[9] Cleveland Clin, Cleveland, OH 44106 USA
[10] Houston Methodist Hosp, Houston, TX USA
关键词
INFORMED-CONSENT; VALIDATION; SATISFACTION; PLACEMENT; HEART; LIFE;
D O I
10.1016/j.cardfail.2018.08.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Studies indicate that decision making and informed consent among patients considering left ventricular assist device (LVAD) support for advanced heart failure could be improved. In the VADDA (Ventricular Assist Device Decision Aid) trial, we tested a patient-centered decision aid (DA) to enhance the quality of decision making about LVAD therapy. Methods: After an extensive user-centered design process, we conducted a multisite randomized trial of the DA compared with standard education (SE) among inpatients considering LVAD treatment for advanced heart failure The main outcome was LVAD knowledge at 1 week and 1 month after administration of the DA versus the SE, according to a validated scale. Secondary measures included prespecified quality decision making measures recommended by the International Patient Decision Aid Standards collaboration. Results: Of 105 eligible patients, 98 consented and were randomly assigned to the DA and SE arms. Patients receiving the VADDA exhibited significantly greater LVAD knowledge than the SE group at 1 week of follow-up (P = .01) but not at 1 month (P = .47). No differences were found between DA and SE patients in rates of acceptance versus decline of LVAD treatment (85% vs 78%; P = .74). Recipients in the DA arm reported greater satisfaction with life after implantation compared with nonrecipients (28 vs 23 out of 30; P = .008), although both arms reported high satisfaction. Patients rated the DA high in acceptability and usability. Conclusions: The VADDA enhances LVAD knowledge, particularly in the short term (1 week) during the peak period of decision making. The DA does not encourage decision direction and reflects patient, care-giver, and physician preferences for content and format.
引用
收藏
页码:661 / 671
页数:11
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